TW200407322A - Novel imidazopyridines as cyclin dependent kinase inhibitors - Google Patents
Novel imidazopyridines as cyclin dependent kinase inhibitorsInfo
- Publication number
- TW200407322A TW200407322A TW092125636A TW92125636A TW200407322A TW 200407322 A TW200407322 A TW 200407322A TW 092125636 A TW092125636 A TW 092125636A TW 92125636 A TW92125636 A TW 92125636A TW 200407322 A TW200407322 A TW 200407322A
- Authority
- TW
- Taiwan
- Prior art keywords
- compounds
- cyclin dependent
- kinase inhibitors
- dependent kinase
- methods
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
In its many embodiments, the present invention provides a novel class of imidazo[1,2-a]pyridine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41206302P | 2002-09-19 | 2002-09-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
TW200407322A true TW200407322A (en) | 2004-05-16 |
TWI351405B TWI351405B (en) | 2011-11-01 |
Family
ID=32030794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW092125636A TWI351405B (en) | 2002-09-19 | 2003-09-17 | Novel imidazopyridines as cyclin dependent kinase |
Country Status (19)
Country | Link |
---|---|
US (2) | US6992080B2 (en) |
EP (1) | EP1539756B1 (en) |
JP (1) | JP4845379B2 (en) |
KR (1) | KR20050052500A (en) |
CN (1) | CN100549011C (en) |
AR (1) | AR041291A1 (en) |
AT (1) | ATE378336T1 (en) |
AU (1) | AU2003295332B2 (en) |
CA (1) | CA2499639C (en) |
DE (1) | DE60317529T2 (en) |
ES (1) | ES2293068T3 (en) |
HK (1) | HK1071757A1 (en) |
IL (1) | IL167433A (en) |
MX (1) | MXPA05003058A (en) |
MY (1) | MY133311A (en) |
NZ (1) | NZ538566A (en) |
TW (1) | TWI351405B (en) |
WO (1) | WO2004026867A2 (en) |
ZA (1) | ZA200502278B (en) |
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JP4579351B2 (en) | 1996-12-03 | 2010-11-10 | スローン−ケッタリング インスティトュート フォア キャンサー リサーチ | Synthesis of epothilone and its intermediates and analogs and uses thereof |
US20040037818A1 (en) * | 1998-07-30 | 2004-02-26 | Brand Stephen J. | Treatment for diabetes |
GB9819530D0 (en) | 1998-09-09 | 1998-10-28 | Smithkline Beecham Plc | Novel compositions and use |
US20020058286A1 (en) * | 1999-02-24 | 2002-05-16 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto and analogues thereof |
ES2204295B1 (en) * | 2002-07-02 | 2005-08-01 | Almirall Prodesfarma, S.A. | NEW DERIVATIVES OF QUINUCLIDINE-AMIDE. |
DK1767535T3 (en) | 2002-08-23 | 2010-04-12 | Sloan Kettering Inst Cancer | Synthesis of epothilones, their intermediates, analogs and their use |
US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
NZ544756A (en) | 2003-07-22 | 2009-09-25 | Astex Therapeutics Ltd | 3,4-Disubstituted 1H-pyrazole compounds and their use as cyclin dependent kinases (CDK) and glycogen synthase kinase-3 (GSK-3) modulators |
GB0418328D0 (en) * | 2004-08-17 | 2004-09-22 | Imp College Innovations Ltd | Cancer methods and medicaments |
US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
BRPI0606480A (en) * | 2005-01-21 | 2008-03-11 | Astex Therapeutics Ltd | pharmaceutical compounds |
MX2007008781A (en) * | 2005-01-21 | 2007-09-11 | Astex Therapeutics Ltd | Pharmaceutical compounds. |
CN101146533A (en) * | 2005-01-21 | 2008-03-19 | 阿斯泰克斯治疗有限公司 | Combinations of pyrazole kinase inhibitors and further antitumor agents |
AR054425A1 (en) | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO. |
WO2006100119A1 (en) * | 2005-03-24 | 2006-09-28 | Glaxo Group Limited | Derivatives of imidazo (1,2-a) pyridine useful as medicaments for treating gastrointestinal diseases |
WO2007032936A2 (en) * | 2005-09-09 | 2007-03-22 | Schering Corporation | Azafused cyclin dependent kinase inhibitors |
US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
KR20080103996A (en) | 2006-02-16 | 2008-11-28 | 쉐링 코포레이션 | Pyrrolidine derivatives as erk inhibitors |
US20090142337A1 (en) * | 2006-05-08 | 2009-06-04 | Astex Therapeutics Limited | Pharmaceutical Combinations of Diazole Derivatives for Cancer Treatment |
FR2906250B1 (en) * | 2006-09-22 | 2008-10-31 | Sanofi Aventis Sa | DERIVATIVES OF 2-ARYL-6PHENYL-IMIDAZO (1,2-A) PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
EP2099798A1 (en) * | 2006-12-01 | 2009-09-16 | Galapagos N.V. | Imidazolopyridine compounds useful for the treatment of degenerative and inflammatory diseases |
CA2672213C (en) | 2006-12-22 | 2016-02-16 | Astex Therapeutics Limited | Bicyclic amine derivatives as protein tyrosine kinase inhibitors |
AU2007337886C1 (en) | 2006-12-22 | 2014-10-16 | Astex Therapeutics Limited | Bicyclic heterocyclic compounds as FGFR inhibitors |
TWI428132B (en) | 2007-07-02 | 2014-03-01 | Lilly Co Eli | Potentiation of cancer chemotherapy |
GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
ES2462642T3 (en) * | 2007-12-14 | 2014-05-26 | F. Hoffmann-La Roche Ag | New derivatives of imidazo [1,2-a] pyridine and imidazo [1,2-b] pyridazine |
US8426441B2 (en) | 2007-12-14 | 2013-04-23 | Roche Palo Alto Llc | Inhibitors of bruton's tyrosine kinase |
PL2222675T3 (en) * | 2007-12-19 | 2014-02-28 | Genentech Inc | 5-anilinoimidazopyridines and methods of use |
US20090221612A1 (en) | 2008-02-13 | 2009-09-03 | Mitchell Scott A | Certain substituted amides, method of making, and method of use thereof |
RU2525389C2 (en) | 2008-02-21 | 2014-08-10 | Мерк Шарп И Доум Корп. | Compounds which are erk inhibitors |
GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
WO2009155388A1 (en) | 2008-06-20 | 2009-12-23 | Bristol-Myers Squibb Company | Imidazopyridine and imidazopyrazine compounds useful as kinase inhibitors |
WO2010006947A1 (en) | 2008-07-15 | 2010-01-21 | F. Hoffmann-La Roche Ag | Novel phenyl-imidazopyridines and pyridazines |
US20110178041A1 (en) * | 2008-09-25 | 2011-07-21 | Yasushi Kohno | Heterocyclic biaryl derivative and pde inhibitor comprising same as active ingredient |
WO2010068258A1 (en) | 2008-12-08 | 2010-06-17 | Cgi Pharmaceuticals, Inc. | Imidazopyrazine syk inhibitors |
VN28228A1 (en) | 2008-12-08 | 2011-12-26 | Gilead Connecticut Inc | Imidazopyrazine Syk inhibitors |
GB0906470D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
ES2651296T3 (en) | 2009-10-30 | 2018-01-25 | Janssen Pharmaceutica, N.V. | Imidazo [1,2-b] pyridacin derivatives and their use as PDE10 inhibitors |
AR080754A1 (en) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | IMIDAZO DERIVATIVES (1,2-A) PIRAZINA AND ITS USE AS PDE10 INHIBITORS |
AU2011226689B2 (en) * | 2010-03-11 | 2016-09-01 | Kronos Bio, Inc. | Imidazopyridines Syk inhibitors |
CA2832310A1 (en) * | 2011-04-06 | 2012-10-11 | Bayer Intellectual Property Gmbh | Substituted imidazopyridines and intermediates thereof |
MX344600B (en) | 2011-06-27 | 2016-12-20 | Janssen Pharmaceutica Nv | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES. |
US8883819B2 (en) | 2011-09-01 | 2014-11-11 | Irm Llc | Bicyclic heterocycle derivatives for the treatment of pulmonary arterial hypertension |
EP2863909B1 (en) | 2012-06-26 | 2020-11-04 | Janssen Pharmaceutica N.V. | Combinations comprising 4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline compounds as pde 2 inhibitors and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
AU2013289284B2 (en) | 2012-07-09 | 2017-03-30 | Janssen Pharmaceutica Nv | Inhibitors of phosphodiesterase 10 enzyme |
US9073921B2 (en) | 2013-03-01 | 2015-07-07 | Novartis Ag | Salt forms of bicyclic heterocyclic derivatives |
SG11201600378SA (en) | 2013-07-30 | 2016-02-26 | Gilead Connecticut Inc | Formulation of syk inhibitors |
KR101810798B1 (en) | 2013-07-30 | 2017-12-19 | 질레드 코네티컷 인코포레이티드 | Polymorph of syk inhibitors |
CN105764516A (en) | 2013-12-04 | 2016-07-13 | 吉利德科学公司 | Methods for treating cancers |
US9290505B2 (en) | 2013-12-23 | 2016-03-22 | Gilead Sciences, Inc. | Substituted imidazo[1,2-a]pyrazines as Syk inhibitors |
TWI735853B (en) | 2013-12-23 | 2021-08-11 | 美商克洛諾斯生技有限公司 | Syk inhibitors |
KR20170029580A (en) | 2014-07-14 | 2017-03-15 | 길리애드 사이언시즈, 인코포레이티드 | Combinations for treating cancers |
EP3377908B1 (en) | 2015-11-18 | 2020-08-05 | Genzyme Corporation | Biomarker of polycystic kidney disease and uses thereof |
US10196396B2 (en) | 2016-01-14 | 2019-02-05 | Handok Inc. | Compounds antagonizing A3 adenosine receptor, method for preparing them, and medical-use thereof |
CN110198942B (en) | 2017-01-24 | 2022-04-15 | 住友化学株式会社 | Fused heterocyclic compound and composition containing the same |
CN110785419B (en) * | 2017-04-12 | 2024-03-01 | 博雅缉因(北京)生物科技有限公司 | Aromatic hydrocarbon receptor antagonist and application thereof |
TWI778050B (en) * | 2017-04-21 | 2022-09-21 | 美商醫肯納腫瘤學公司 | Indole ahr inhibitors and uses thereof |
KR20220070056A (en) | 2017-08-25 | 2022-05-27 | 길리애드 사이언시즈, 인코포레이티드 | Polymorphs of syk inhibitors |
AU2020225455A1 (en) | 2019-02-22 | 2021-09-09 | Kronos Bio, Inc. | Solid forms of condensed pyrazines as Syk inhibitors |
IL293326A (en) | 2019-11-26 | 2022-07-01 | Ikena Oncology Inc | Polymorphic carbazole derivatives and uses thereof |
WO2024068740A1 (en) * | 2022-09-28 | 2024-04-04 | Origenis Gmbh | Novel cdk9 inhibitors |
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US5574042A (en) * | 1992-11-02 | 1996-11-12 | Fujisawa Pharmaceutical Co., Ltd | Imidazo [1,2-a] pyridines and their pharmaceutical use |
CN1221533C (en) | 1993-09-10 | 2005-10-05 | 卫材株式会社 | Heterobicyclic sulfonamide derivative and sulfonic ester derivative |
AU5348396A (en) * | 1995-05-01 | 1996-11-21 | Fujisawa Pharmaceutical Co., Ltd. | Imidazo 1,2-a pyridine and imidazo 1,2-a pyridezine derivati ves and their use as bone resorption inhibitors |
SE9700661D0 (en) | 1997-02-25 | 1997-02-25 | Astra Ab | New compounds |
SE9801526D0 (en) | 1998-04-29 | 1998-04-29 | Astra Ab | New compounds |
SE9802794D0 (en) * | 1998-08-21 | 1998-08-21 | Astra Ab | New compounds |
JP4007743B2 (en) * | 1999-02-26 | 2007-11-14 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Angiogenesis inhibitor |
HUP0300544A3 (en) * | 2000-02-03 | 2005-03-29 | Eisai Co Ltd | Pharmaceutical compositions containing integrin expression inhibitors |
SE0003186D0 (en) | 2000-09-07 | 2000-09-07 | Astrazeneca Ab | New process |
EE05234B1 (en) * | 2001-03-08 | 2009-12-15 | Astrazeneca Ab | Use of 6-Carboxamidoimidazo [1,2-a] pyridine Compounds to Prevent Drug-Induced Gastric Ulcer |
-
2003
- 2003-09-17 KR KR1020057004361A patent/KR20050052500A/en active IP Right Grant
- 2003-09-17 WO PCT/US2003/029498 patent/WO2004026867A2/en active IP Right Grant
- 2003-09-17 AT AT03786514T patent/ATE378336T1/en not_active IP Right Cessation
- 2003-09-17 MY MYPI20033536A patent/MY133311A/en unknown
- 2003-09-17 EP EP03786514A patent/EP1539756B1/en not_active Expired - Lifetime
- 2003-09-17 CN CNB038250470A patent/CN100549011C/en not_active Expired - Fee Related
- 2003-09-17 DE DE60317529T patent/DE60317529T2/en not_active Expired - Lifetime
- 2003-09-17 MX MXPA05003058A patent/MXPA05003058A/en active IP Right Grant
- 2003-09-17 ES ES03786514T patent/ES2293068T3/en not_active Expired - Lifetime
- 2003-09-17 AU AU2003295332A patent/AU2003295332B2/en not_active Ceased
- 2003-09-17 CA CA2499639A patent/CA2499639C/en not_active Expired - Fee Related
- 2003-09-17 TW TW092125636A patent/TWI351405B/en not_active IP Right Cessation
- 2003-09-17 NZ NZ538566A patent/NZ538566A/en not_active IP Right Cessation
- 2003-09-17 AR ARP030103373A patent/AR041291A1/en not_active Application Discontinuation
- 2003-09-17 JP JP2004538237A patent/JP4845379B2/en not_active Expired - Fee Related
- 2003-09-17 US US10/664,338 patent/US6992080B2/en not_active Expired - Lifetime
-
2005
- 2005-03-15 IL IL167433A patent/IL167433A/en not_active IP Right Cessation
- 2005-03-17 ZA ZA200502278A patent/ZA200502278B/en unknown
- 2005-06-15 HK HK05104993A patent/HK1071757A1/en not_active IP Right Cessation
- 2005-09-29 US US11/238,597 patent/US7452902B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
WO2004026867A3 (en) | 2004-08-05 |
WO2004026867A2 (en) | 2004-04-01 |
ES2293068T3 (en) | 2008-03-16 |
MY133311A (en) | 2007-11-30 |
CA2499639C (en) | 2011-11-08 |
ATE378336T1 (en) | 2007-11-15 |
EP1539756A2 (en) | 2005-06-15 |
CN1703414A (en) | 2005-11-30 |
US20040097517A1 (en) | 2004-05-20 |
AU2003295332B2 (en) | 2007-01-18 |
IL167433A (en) | 2011-03-31 |
EP1539756B1 (en) | 2007-11-14 |
ZA200502278B (en) | 2006-05-31 |
AR041291A1 (en) | 2005-05-11 |
US20060030555A1 (en) | 2006-02-09 |
CA2499639A1 (en) | 2004-04-01 |
MXPA05003058A (en) | 2005-05-27 |
AU2003295332A1 (en) | 2004-04-08 |
DE60317529D1 (en) | 2007-12-27 |
DE60317529T2 (en) | 2008-09-25 |
JP4845379B2 (en) | 2011-12-28 |
JP2006507254A (en) | 2006-03-02 |
TWI351405B (en) | 2011-11-01 |
US6992080B2 (en) | 2006-01-31 |
HK1071757A1 (en) | 2005-07-29 |
CN100549011C (en) | 2009-10-14 |
KR20050052500A (en) | 2005-06-02 |
US7452902B2 (en) | 2008-11-18 |
NZ538566A (en) | 2008-02-29 |
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MM4A | Annulment or lapse of patent due to non-payment of fees |